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dc.contributor.authorArunachalam, Rajendran
dc.contributor.authorChinnaraja, Eswaran
dc.contributor.authorValkonen, Arto
dc.contributor.authorRissanen, Kari
dc.contributor.authorSubramanian, Palani S.
dc.date.accessioned2024-03-04T08:09:05Z
dc.date.available2024-03-04T08:09:05Z
dc.date.issued2019
dc.identifier.citationArunachalam, R., Chinnaraja, E., Valkonen, A., Rissanen, K., & Subramanian, P. S. (2019). Bifunctional coordination polymers as efficient catalysts for carbon dioxide conversion. <i>Applied Organometallic Chemistry</i>, <i>33</i>(11), Article e5202. <a href="https://doi.org/10.1002/aoc.5202" target="_blank">https://doi.org/10.1002/aoc.5202</a>
dc.identifier.otherCONVID_32670915
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/93782
dc.description.abstractThe multidentate ligand H2L upon complexation with Zn (II) and Cd (II) provide a one‐dimensional polymeric networks. These coordination polymers (CPs) CP‐1 and CP‐2 containing Zn (II) and Cd (II) metals respectively are well characterized. The single crystal structural analysis confirms the formation of one‐dimensional coordination polymer with zigzag fashion in CP‐1 and ladder chain CP‐2. Both the CPs are applied as catalysts to synthesize various cyclic carbonates from epoxides and carbon dioxide. The catalysts are giving better conversion under solvent‐free and additive‐free condition using 10 bar CO2 and 100 °C as optimized pressure and temperature. The detailed kinetic experiments suggesting the first order kinetics, the energy of activation (Ea) is calculated for this catalytic conversion.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherJohn Wiley & Sons
dc.relation.ispartofseriesApplied Organometallic Chemistry
dc.rightsIn Copyright
dc.subject.otheractivation energy
dc.subject.otherCO2utilization
dc.subject.othercoordination polymers
dc.subject.othercyclic carbonates
dc.subject.otherreaction kinetics
dc.titleBifunctional coordination polymers as efficient catalysts for carbon dioxide conversion
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202403042249
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0268-2605
dc.relation.numberinseries11
dc.relation.volume33
dc.type.versionacceptedVersion
dc.rights.copyright© 2019 John Wiley & Sons, Ltd.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber314343
dc.subject.ysokemialliset reaktiot
dc.subject.ysopolymeerit
dc.subject.ysohiilidioksidi
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p3658
jyx.subject.urihttp://www.yso.fi/onto/yso/p926
jyx.subject.urihttp://www.yso.fi/onto/yso/p4728
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1002/aoc.5202
dc.relation.funderSuomen Akatemiafi
dc.relation.funderResearch Council of Finlanden
jyx.fundingprogramAkatemiatutkijan tutkimuskulut, SAfi
jyx.fundingprogramResearch costs of Academy Research Fellow, AoFen
jyx.fundinginformationCSMCRI communication number 006/2019. R. A and E. C acknowledge CSIR for SRF and Indus Magic project no CSC‐0123 for financial assistance. Dr. S. Kannan is greatly acknowledged for the reactor facilities to perform this work. Dr. E. Suresh is acknowledged for his assistance of single crystal description. Dr. P. S acknowledges the CSIR for Indus Magic Project No. CSC‐0123 and DST‐SERB New Delhi (project No SR/S1/IC‐23/2011) for financial support. A. V. also kindly acknowledges the Academy of Finland (grant no. 314343) for financial support. We are thankful to ADCIF for the instrument support.
dc.type.okmA1


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